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口腔支原体(一种常见的细胞培养污染物)对淋巴细胞增殖的刺激作用。

Stimulation of lymphoid cell proliferation by Mycoplasma orale, a common cell culture contaminant.

作者信息

Mizushima Y, Quintans J, Cohen E P

出版信息

Infect Immun. 1985 Dec;50(3):636-40. doi: 10.1128/iai.50.3.636-640.1985.

Abstract

Mycoplasma orale, maintained as a contaminant of a mouse hybrid cell line, induces an intense proliferation in short-term culture of lymphoid cells of inbred mice. Cell division induced by the contaminated cell culture fluid reaches a maximum on day four and declines rapidly thereafter. Culture fluids from hybrid cells freed of contamination do not cause proliferation. Cells from the spleen, bone marrow, and thymus of each of several strains of inbred mice, including xid CBA/N, poorly responsive to lipopolysaccharide, are stimulated by the mitogen, as are cells from BALB/c nude mice. The characteristics of the stimulatory effect are analogous in several important aspects to those of naturally occurring T cell-derived growth factors. In the absence of detectable numbers of T cells, both small and large B lymphocytes undergo mitosis in the presence of contaminated cell culture fluid, and B cells stimulated to divide by lipopolysaccharide are sustained for further rounds of replication by M. orale-containing cell culture fluid. The fluid also augments the stimulatory effect on thymocytes of suboptimum concentrations of phytohemagglutinin mimicking the effect of interleukin-1. Unlike with most naturally occurring lymphoid cell mitogens, however, the dividing cells do not go on to immunoglobulin secretion.

摘要

口腔支原体作为小鼠杂交细胞系的污染物被保存下来,它能在近交系小鼠淋巴细胞的短期培养中诱导强烈增殖。受污染的细胞培养液诱导的细胞分裂在第四天达到最大值,此后迅速下降。去除污染的杂交细胞的培养液不会引起增殖。包括对脂多糖反应较差的xid CBA/N在内的几种近交系小鼠的脾脏、骨髓和胸腺细胞,以及BALB/c裸鼠的细胞,都受到该有丝分裂原的刺激。刺激作用的特征在几个重要方面与天然存在的T细胞衍生生长因子的特征相似。在检测不到T细胞数量的情况下,无论大小B淋巴细胞在受污染的细胞培养液存在时都会进行有丝分裂,并且被脂多糖刺激分裂的B细胞会被含口腔支原体的细胞培养液维持进行进一步的复制轮次。该培养液还增强了亚最佳浓度植物血凝素对胸腺细胞的刺激作用,模拟了白细胞介素-1的作用。然而,与大多数天然存在的淋巴细胞有丝分裂原不同,分裂的细胞不会继续分泌免疫球蛋白。

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Stimulation of lymphoid cell proliferation by Mycoplasma orale, a common cell culture contaminant.
Infect Immun. 1985 Dec;50(3):636-40. doi: 10.1128/iai.50.3.636-640.1985.

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